MiR-29a mediates the apoptotic effects of TNF-α on endothelial cells through inhibiting PI3K/AKT/BCL-2 axis.

Endothelial cell apoptosis driven by inflammation (TNF-α) plays a critical role in the pathogenesis of atherosclerosis, but the exact molecular mechanisms are not clearly elucidated. MicroRNA (miR)-29 families (a/b/c) take important roles in pathophysiological processes of atherosclerosis, also the underlying mechanisms have not been fully clarified. The aims are to explore whether or not miR-29 families mediate the apoptotic effects of TNF-α on endothelial cells and uncover the underlying molecular mechanisms. In this study, MTT assay and flow cytometer analysis were employed respectively to determine the proliferation and apoptosis of human umbilical vascular endothelial cells (HUVECs) under TNF-α exposure. Real-time quantitative PCR and western blot were performed to detect the levels of target RNAs and proteins/their phosphorylation in HUVECs. TNF-α could inhibit HUVEC proliferation and induce HUVEC apoptosis in a positive dose- and time-dependent manner, with a similar way of miR-29a upregulation, but no effects on miR-29b/c. Upregulation of miR-29a with its mimics enhanced the apoptotic effect of TNF-α on HUVECs, but downregulation of miR-29a using anti-miR-29a blocked up its apoptotic effect. MiR-29a inhibited the expression of PI3Kp85α and Bcl-2 and blocked up the signal transduction of PI3K/AKT/Bcl-2 axis to mediate the apoptotic effect of TNF-α on HUVECs. Mediating the inflammation-driven endothelial cell apoptosis is an important biology mechanism by which miR-29a promotes atherosclerosis and its complications. MiR-29a will be a potential diagnostic and therapeutic target for atherosclerotic cardiovascular diseases; it is worthwhile to further study.

SiNPs induce ferroptosis in HUVECs through p38 inhibiting NrF2 pathway.

Introduction: Despite of growing evidence linking silica nanoparticles (SiNPs), one of the global-top-three-produced and -used nanoparticle (NP), to human health risks, there remain many knowledge gaps over the adverse effects of SiNPs exposure on cardiovascular system and the underlying molecular mechanisms. Methods: In this study, the ferroptotic effects of SiNPs (20 nm; 0, 25, 50, and 100 µg/mL) on human umbilical vein endothelial cells (HUVECs) and the possible molecular mechanism were studied with the corresponding biochemical and molecular biology assays. Results and discussion: The results showed that at the tested concentrations, SiNPs could decrease HUVEC viability, but the deferoxamine mesylate (an iron ion chelator) might rescue this reduction of cell viability. Also, increased levels of intracellular reactive oxygen species and enhanced mRNA expression of lipid oxidation enzymes (ACSL4 and LPCAT3) with increase in lipid peroxidation (malondialdehyde), but decreased ratios of intracellular GSH/total-GSH and mitochondrial membrane potential as well as reduced enzymatic activities of anti-oxidative enzymes (CAT, SOD, and GSH-PX), were found in the SiNPs-treated HUVECs. Meanwhile, increase in p38 protein phosphorylation and decrease in NrF2 protein phosphorylation with reduced mRNA expressions of downstream anti-oxidative enzyme genes (CAT, SOD1, GSH-PX, and GPX4) was identified in the SiNPs-exposed HUVECs. These data indicated that SiNPs exposure might induce ferroptosis in HUVECs via p38 inhibiting NrF2 pathway. Ferroptosis of HUVECs will become a useful biomarker for assessing the cardiovascular health risks of environmental contaminants.

The pathophysiological and molecular mechanisms of atmospheric PM2.5 affecting cardiovascular health: A review.

BACKGROUND: Exposure to ambient fine particulate matter (PM2.5, with aerodynamic diameter less than 2.5 µm) is a leading environmental risk factor for global cardiovascular health concern. OBJECTIVE: To provide a roadmap for those new to this field, we reviewed the new insights into the pathophysiological and cellular/molecular mechanisms of PM2.5 responsible for cardiovascular health. MAIN FINDINGS: PM2.5 is able to disrupt multiple physiological barriers integrity and translocate into the systemic circulation and get access to a range of secondary target organs. An ever-growing body of epidemiological and controlled exposure studies has evidenced a causal relationship between PM2.5 exposure and cardiovascular morbidity and mortality. A variety of cellular and molecular biology mechanisms responsible for the detrimental cardiovascular outcomes attributable to PM2.5 exposure have been described, including metabolic activation, oxidative stress, genotoxicity, inflammation, dysregulation of Ca2+ signaling, disturbance of autophagy, and induction of apoptosis, by which PM2.5 exposure impacts the functions and fates of multiple target cells in cardiovascular system or related organs and further alters a series of pathophysiological processes, such as cardiac autonomic nervous system imbalance, increasing blood pressure, metabolic disorder, accelerated atherosclerosis and plaque vulnerability, platelet aggregation and thrombosis, and disruption in cardiac structure and function, ultimately leading to cardiovascular events and death. Therein, oxidative stress and inflammation were suggested to play pivotal roles in those pathophysiological processes. CONCLUSION: Those biology mechanisms have deepen insights into the etiology, course, prevention and treatment of this public health concern, although the underlying mechanisms have not yet been entirely clarified.

Uranium induces kidney cells pyroptosis in culture involved in ROS/NLRP3/caspase-1 signaling.

Pyroptosis is an exceptional mode of inflammation and programmed cell death involved in inflammasomes and Caspase-1 activation and inflammatory cytokines releasing. Our goal is to explore whether uranium (U)-intoxication could induce NRK-52E cells pyroptosis in vitro and its underlying molecular mechanism. Rat NRK-52E cells were intoxicated with U concentrations (400-500 µM) for 24 h. The results indicate that the cells showed characteristic features of pyroptosis, which were identified through augmented NLRP3 and cleaved Caspase-1 proteins expression, GSDMD mRNA level, mature interleukin IL-18 and IL-1ß contents, LDH leakage, and the number of double-positive cells. But, administration of glycine (an inhibitor of pyroptosis) effectively attenuated U-induced pyroptosis, LDH releasing and cytotoxicity. Pretreatment of CRID3 (an inhibitor of NLRP3 inflammasome) evidently abrogated NLRP3 and cleaved Caspase-1 proteins and GSDMD mRNA expression which all were up-regulated by U exposure. Simultaneously, CRID3 significantly reversed U-increased pyroptosis rate and active interleukin IL-18 and IL-1ß contents. NAC application (an ROS scavenger) effectively decreased U-increased ROS content and NLRP3 expression and restored U-induced pyroptosis. Taken together, our results suggest that U-treatment can trigger NRK-52E cells pyroptosis which is involvement of ROS/NLRP3/Caspase-1 pathway. Targeting ROS/NLRP3/Caspase-1-mediated pyroptosis may be a novel approach for attenuating U nephrotoxicity.

Intercomparison of Soil Moisture Retrieved from GNSS-R and from Passive L-Band Radiometry at the Valencia Anchor Station.

In this paper, the SOMOSTA (Soil Moisture Monitoring Station) experiment on the intercomparison of soil moisture monitoring from Global Navigation Satellite System Reflectometry (GNSS-R) signals and passive L-band microwave radiometer observations at the Valencia Anchor Station is introduced. The GNSS-R instrument has an up-looking antenna for receiving direct signals from satellites, and a dual-pol down-looking antenna for receiving LHCP (left-hand circular polarization) and RHCP (right-hand circular polarization) reflected signals from the soil surface. Data were collected from the three different antennas through the two channels of Oceanpal GNSS-R receiver and, in addition, calibration was performed to reduce the impact from the differing channels. Reflectivity was thus measured, and soil moisture could be retrieved. The ESA (European Space Agency)-funded ELBARA-II (ESA L Band Radiometer II) is an L-band radiometer with two channels with 11 MHz bandwidth and respective center frequencies of 1407.5 MHz and 1419.5 MHz. The ELBARAII antenna is a large dual-mode Picket horn that is 1.4 m wide, with a length of 2.7 m with -3 dB full beam width of 12° (±6° around the antenna main direction) and a gain of 23.5 dB. By comparing GNSS-R and ELBARA-II radiometer data, a high correlation was found between the LHCP reflectivity measured by GNSS-R and the horizontal/vertical reflectivity from the radiometer (with correlation coefficients ranging from 0.83 to 0.91). Neural net fitting was used for GNSS-R soil moisture inversion, and the RMSE (Root Mean Square Error) was 0.014 m3/m3. The determination coefficient between the retrieved soil moisture and in situ measurements was R2 = 0.90 for Oceanpal and R2 = 0.65 for Elbara II, and the ubRMSE (Unbiased RMSE) were 0.0128 and 0.0734 respectively. The soil moisture retrievals by both L-band remote sensing methods show good agreement with each other, and their mutual correspondence with in-situ measurements and with rainfall was also good.